Package 72657-109-01

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 72657-109-01
Digits Only 7265710901
Product NDC 72657-109
Product ID 72657-109_c5c89eef-6b45-4dc7-8c88-89d972a3e4b5
Description

100 TABLET, FILM COATED in 1 BOTTLE (72657-109-01)

Marketing

Marketing Status
Marketed Since 2022-01-13
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c5c89eef-6b45-4dc7-8c88-89d972a3e4b5", "openfda": {"upc": ["0372657111010", "0372657109017", "0372657110013"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["18330b41-27ad-461b-a0a9-aac94e8ee87f"], "manufacturer_name": ["Glenmark Therapeutics Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72657-109-01)", "package_ndc": "72657-109-01", "marketing_start_date": "20220113"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72657-109-05)", "package_ndc": "72657-109-05", "marketing_start_date": "20220113"}], "brand_name": "Citalopram Hydrobromide", "product_id": "72657-109_c5c89eef-6b45-4dc7-8c88-89d972a3e4b5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72657-109", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Glenmark Therapeutics Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077654", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}